lansoprazole
- Product NDC
- 41250-117
- 11-digit product format
- 412500117
- Labeler code
- 41250
- Product ID
- 41250-117_c7df2594-5fe3-455f-896a-92797c0f14e2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2012-05-18
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-117-01 | 41250011701 | 1 BOTTLE in 1 CARTON (41250-117-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2012-05-18 | 0000-00-00 | No | No | Current |
| 41250-117-03 | 41250011703 | 3 BOTTLE in 1 CARTON (41250-117-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2012-05-18 | 0000-00-00 | No | No | Current |